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Absence of mucosal-associated invariant T cells in a person with a homozygous point mutation in MR1

Authors :
Abdul Rezzak Hamzeh
Hui Jing Lim
T. Andrews
Lauren J. Howson
David H. McDermott
Philip M. Murphy
Jérôme Le Nours
Matthew C. Cook
Ligong Liu
Jamie Rossjohn
Martin S. Davey
Stephen J. Turner
James McCluskey
Jeffrey Y. W. Mak
Maria L. Sandoval-Romero
Shamik Majumdar
Wael Awad
Anouk von Borstel
Hamish E G McWilliam
Samar Ojaimi
David P. Fairlie
Jose A Villadangos
Source :
Sci Immunol
Publication Year :
2020

Abstract

The role unconventional T cells play in protective immunity in humans is unclear. Mucosal-associated invariant T (MAIT) cells are an unconventional T cell subset restricted to the antigen-presenting molecule MR1. Here, we report the discovery of a patient homozygous for a rare Arg31His (R9H in the mature protein) mutation in MR1 who has a history of difficult-to-treat viral and bacterial infections. MR1R9H was unable to present the potent microbially derived MAIT cell stimulatory ligand. The MR1R9H crystal structure revealed that the stimulatory ligand cannot bind due to the mutation lying within, and causing structural perturbation to, the ligand-binding domain of MR1. While MR1R9H could bind and be up-regulated by a MAIT cell inhibitory ligand, the patient lacked circulating MAIT cells. This shows the importance of the stimulatory ligand for MAIT cell selection in humans. The patient had an expanded γδ T cell population, indicating a compensatory interplay between these unconventional T cell subsets.

Details

Language :
English
Database :
OpenAIRE
Journal :
Sci Immunol
Accession number :
edsair.doi.dedup.....d528ed38c4afdc498bf2a10180500870